Canonical Allele Identifier: CA401670681

Gene: TYMS

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.669174G>A , CM000680.2:g.669174G>A	GRCh38
NC_000018.9:g.669174G>A , CM000680.1:g.669174G>A	GRCh37
NC_000018.8:g.659174G>A	NCBI36
NG_028255.1:g.16571G>A , LRG_783:g.16571G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001071.4:c.556+1G>A MANE Select	NP_001062.1:n.556+1G>A
ENST00000323274.15:c.556+1G>A MANE Select	ENSP00000315644.10:n.556+1G>A
NM_001071.2:c.556+1G>A , LRG_783t1:c.556+1G>A	NP_001062.1:n.556+1G>A
NM_001071.3:c.556+1G>A	NP_001062.1:n.556+1G>A
NM_001354867.1:c.455-1518G>A	NP_001341796.1:n.455-1518G>A
NM_001354867.2:c.455-1518G>A	NP_001341796.1:n.455-1518G>A
NM_001354868.1:c.307+1G>A	NP_001341797.1:n.307+1G>A
NM_001354868.2:c.307+1G>A	NP_001341797.1:n.307+1G>A
ENST00000323224.7:c.455-1518G>A	ENSP00000314727.7:n.455-1518G>A
ENST00000323250.9:c.307+1G>A	ENSP00000314902.5:n.307+1G>A
ENST00000323274.14:c.556+1G>A	ENSP00000315644.10:n.556+1G>A
ENST00000579128.1:n.635G>A
ENST00000581920.1:n.134+1G>A
XM_024451242.1:c.175+1G>A	XP_024307010.1:n.175+1G>A